DNA conformation-dependent activities of human mitochondrial RNA polymerase

被引:19
作者
Fukuoh, Atsushi [1 ]
Ohgaki, Kippei [1 ]
Hatae, Hinako [1 ]
Kuraoka, Isao [2 ]
Aoki, Yoshimasa [1 ]
Uchiumi, Takeshi [1 ]
Jacobs, Howard T. [3 ,4 ]
Kang, Dongchon [1 ]
机构
[1] Kyushu Univ, Grad Sch Med Sci, Dept Clin Chem & Lab Med, Fukuoka 8128582, Japan
[2] Osaka Univ, Grad Sch Engn Sci, Toyonaka, Osaka 5608531, Japan
[3] Univ Tampere, Tampere Univ Hosp, FI-33014 Tampere, Finland
[4] Univ Tampere, Inst Med Technol, FI-33014 Tampere, Finland
基金
芬兰科学院;
关键词
TRANSCRIPTION-FACTOR-A; MTDNA COPY NUMBER; LAGGING-STRAND; MAMMALIAN MITOCHONDRIA; DISPLACEMENT LOOP; BINDING PROTEIN; TERMINAL TAIL; REPLICATION; TFAM; MAINTENANCE;
D O I
10.1111/j.1365-2443.2009.01328.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mitochondrial RNA polymerase (POLRMT) is a core protein for mitochondrial DNA (mtDNA) transcription. In addition, POLRMT is assumed to be involved in replication, although its exact role is not yet clearly elucidated. We have found novel properties of human POLRMT using a reconstituted transcription system. Various lengths of RNA molecules were synthesized from templates even without a defined promoter sequence, when we used supercoiled circular double-stranded DNA as a template. This promoter-independent activity was as strong as the promoter-dependent one. Promoter-independent DNA conformation-dependent transcription required TFB2M. On supercoiled templates, the promoter-independent activity was strongly suppressed by a putatively physiological amount of TFAM, while promoter-dependent transcription was inhibited to a lesser extent. These different inhibition patterns by TFAM may be important for prevention of random RNA synthesis in vivo. Promoter-independent activity was also observed on relaxed circular single-stranded DNA, where its activity no longer required TFB2M. RNA synthesis on single-stranded DNA was weakly suppressed by a putatively physiological amount of TFAM but restored by the addition of mitochondrial single-stranded DNA binding protein. We suggest that these properties of POLRMT could explain the characteristic features of mammalian mtDNA transcription and replication.
引用
收藏
页码:1029 / 1042
页数:14
相关论文
共 39 条
[1]   Human mitochondrial DNA is packaged with TFAM [J].
Alam, TI ;
Kanki, T ;
Muta, T ;
Ukaji, K ;
Abe, Y ;
Nakayama, H ;
Takio, K ;
Hamasaki, N ;
Kang, DC .
NUCLEIC ACIDS RESEARCH, 2003, 31 (06) :1640-1645
[2]   PRESENCE OF DNA MOLECULES WITH A DISPLACEMENT LOOP IN STANDARD MITOCHONDRIAL DNA PREPARATIONS [J].
ARNBERG, A ;
VANBRUGG.EF ;
TERSCHEG.J ;
BORST, P .
BIOCHIMICA ET BIOPHYSICA ACTA, 1971, 246 (02) :353-&
[3]   Mitochondrial transcription and its regulation in mammalian cells [J].
Asin-Cayuela, Jordi ;
Gustafsson, Claes M. .
TRENDS IN BIOCHEMICAL SCIENCES, 2007, 32 (03) :111-117
[4]  
BAPTISTE J, 1993, PCR PROTOCOLS CURREN
[5]   Mammalian mitochondrial DNA replicates bidirectionally from an initiation zone [J].
Bowmaker, M ;
Yang, MY ;
Yasukawa, T ;
Reyes, A ;
Jacobs, HT ;
Huberman, JA ;
Holt, IJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (51) :50961-50969
[6]   PREFERENCE OF HUMAN MITOCHONDRIAL RNA-POLYMERASE FOR SUPERHELICAL TEMPLATES WITH MITOCHONDRIAL PROMOTERS [J].
BUZAN, JM ;
LOW, RL .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 152 (01) :22-29
[7]   PRIMING OF HUMAN MITOCHONDRIAL-DNA REPLICATION OCCURS AT THE LIGHT-STRAND PROMOTER [J].
CHANG, DD ;
CLAYTON, DA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (02) :351-355
[8]   REPLICATION AND TRANSCRIPTION OF VERTEBRATE MITOCHONDRIAL-DNA [J].
CLAYTON, DA .
ANNUAL REVIEW OF CELL BIOLOGY, 1991, 7 :453-478
[9]   Relative abundance of the human mitochondrial transcription system and distinct roles for h-mtTFB1 and h-mtTFB2 in mitochondrial biogenesis and gene expression [J].
Cotney, Justin ;
Wang, Zhibo ;
Shadel, Gerald S. .
NUCLEIC ACIDS RESEARCH, 2007, 35 (12) :4042-4054
[10]   ADDITION OF A 29-RESIDUE CARBOXYL-TERMINAL TAIL CONVERTS A SIMPLE HMG BOX-CONTAINING PROTEIN TRANSCRIPTIONAL ACTIVATOR [J].
DAIRAGHI, DJ ;
SHADEL, GS ;
CLAYTON, DA .
JOURNAL OF MOLECULAR BIOLOGY, 1995, 249 (01) :11-28